JPS6147175B2 - - Google Patents
Info
- Publication number
- JPS6147175B2 JPS6147175B2 JP5006379A JP5006379A JPS6147175B2 JP S6147175 B2 JPS6147175 B2 JP S6147175B2 JP 5006379 A JP5006379 A JP 5006379A JP 5006379 A JP5006379 A JP 5006379A JP S6147175 B2 JPS6147175 B2 JP S6147175B2
- Authority
- JP
- Japan
- Prior art keywords
- general formula
- lower alkyl
- alkyl group
- formula
- naphtholactam
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000003054 catalyst Substances 0.000 claims description 14
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- -1 inorganic acid halide Chemical class 0.000 claims description 12
- 239000002184 metal Substances 0.000 claims description 9
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 238000006482 condensation reaction Methods 0.000 claims description 5
- 239000011521 glass Substances 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 3
- 239000000981 basic dye Substances 0.000 claims description 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 238000005260 corrosion Methods 0.000 claims description 3
- 230000007797 corrosion Effects 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 229920003002 synthetic resin Polymers 0.000 claims description 3
- 239000000057 synthetic resin Substances 0.000 claims description 3
- 150000001450 anions Chemical class 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 description 14
- 150000001875 compounds Chemical class 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 239000000975 dye Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- GPYLCFQEKPUWLD-UHFFFAOYSA-N 1h-benzo[cd]indol-2-one Chemical compound C1=CC(C(=O)N2)=C3C2=CC=CC3=C1 GPYLCFQEKPUWLD-UHFFFAOYSA-N 0.000 description 1
- KHABYXGVKDDLGT-UHFFFAOYSA-N 6-bromo-1-ethylbenzo[cd]indol-2-one Chemical compound C1=CC(N(CC)C2=O)=C3C2=CC=CC3=C1Br KHABYXGVKDDLGT-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
- PHSPJQZRQAJPPF-UHFFFAOYSA-N N-alpha-Methylhistamine Chemical compound CNCCC1=CN=CN1 PHSPJQZRQAJPPF-UHFFFAOYSA-N 0.000 description 1
- 239000001045 blue dye Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- DVHTZYZBKUFUOA-UHFFFAOYSA-N n-(2-ethoxyethyl)-n-ethylaniline Chemical compound CCOCCN(CC)C1=CC=CC=C1 DVHTZYZBKUFUOA-UHFFFAOYSA-N 0.000 description 1
- MKEXQAIUIWQDQV-UHFFFAOYSA-N n-(2-ethoxyethyl)-n-methylaniline Chemical compound CCOCCN(C)C1=CC=CC=C1 MKEXQAIUIWQDQV-UHFFFAOYSA-N 0.000 description 1
- IBRLRCIVUSLMRB-UHFFFAOYSA-N n-(2-methoxyethyl)-n-methylaniline Chemical compound COCCN(C)C1=CC=CC=C1 IBRLRCIVUSLMRB-UHFFFAOYSA-N 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- UXCDUFKZSUBXGM-UHFFFAOYSA-N phosphoric tribromide Chemical compound BrP(Br)(Br)=O UXCDUFKZSUBXGM-UHFFFAOYSA-N 0.000 description 1
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5006379A JPS55142056A (en) | 1979-04-23 | 1979-04-23 | Preparation of basic dye |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5006379A JPS55142056A (en) | 1979-04-23 | 1979-04-23 | Preparation of basic dye |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS55142056A JPS55142056A (en) | 1980-11-06 |
| JPS6147175B2 true JPS6147175B2 (enrdf_load_stackoverflow) | 1986-10-17 |
Family
ID=12848530
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5006379A Granted JPS55142056A (en) | 1979-04-23 | 1979-04-23 | Preparation of basic dye |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS55142056A (enrdf_load_stackoverflow) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4369188A (en) * | 1981-07-17 | 1983-01-18 | Ayerst, Mckenna & Harrison Inc. | 2-Thioxobenz[cd]indole-1(2H)-acetic acid derivatives |
-
1979
- 1979-04-23 JP JP5006379A patent/JPS55142056A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS55142056A (en) | 1980-11-06 |
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